Experienced Study Start-Up Research Coordinator

Responsibilities

• Communicate with research sites to collect all essential documents required before the site begins to screen patients to participate in the clinical trial.
• Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF).
• Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards).
• Maintain timelines for study start-up through both internal and external collaboration.
• Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements.
• Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges.

Qualifications

• A minimum of a Bachelor's degree in a Life Sciences field (preferable).
• Experience as a Clinical Research Coordinator or industry equivalent (minimum 3 years).
• Excellent organizational and prioritization skills.
• Experience with Institutional Review Board (IRB) submissions and Informed Consent Form development is required.
• Knowledge of Microsoft Office.
• Great attention to detail and excellent oral and written communication skills.

Pay

A target salary range of $40,000 - $100,000 with potential for bonus awards. Your compensation will be based on your skills and experience.

Benefits

• Medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations).

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Denver Perks

• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Structured career paths with opportunities for professional growth
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Road Trip Pass
• Secure bike storage room

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.